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Childrens Mucinex Cough
Childrens Mucinex Cough - 63824-281-64 - (GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE)
Drug Information of Childrens Mucinex Cough
| Product NDC: | 63824-281 |
| Proprietary Name: | Childrens Mucinex Cough |
| Non Proprietary Name: | GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE |
| Active Ingredient(s): | 5; 100 mg/5mL; mg/5mL & nbsp; GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Mucinex Cough
| Product NDC: | 63824-281 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110701 |
Package Information of Childrens Mucinex Cough
| Package NDC: | 63824-281-64 |
| Package Description: | 1 BOTTLE in 1 CARTON (63824-281-64) > 118 mL in 1 BOTTLE |
NDC Information of Childrens Mucinex Cough
| NDC Code | 63824-281-64 |
| Proprietary Name | Childrens Mucinex Cough |
| Package Description | 1 BOTTLE in 1 CARTON (63824-281-64) > 118 mL in 1 BOTTLE |
| Product NDC | 63824-281 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 5; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
